Job Description
This Computer Systems Validation Consultant position is responsible for independently managing Computer System Validation related projects and providing consulting and contract services to clients. It will provide basic support to computer system validation activities focusing primarily on verification test execution and limited technical writing. Some co-authorship of industry blogs and white papers on technical topics of current interest is expected.
Essential Functions Include:
- Obtain specific assignments from ProPharma Group or client Project Manager.
- Ensure individual activities are clearly communicated and documented to Project Manager.
- Execute basic qualification protocols (IQ/OQ/PQ), document deviations, and develop traceability matrices.
- Review assigned protocols prior to execution.
- Perform technical writing and communicate clearly on all technical, business, and professional interpersonal levels of the organization.
- Apply Computer System Validation experience as it relates to GxP regulated business processes.
- Attend and contribute to scheduled Practice meetings.
- Participate in company programs such as Project Management, Quality, Social Responsibility, Wellness, Safety and Training.
- Create annual personal goals and development plan with administrative manager.
- Assist with interviews of ProPharma Group candidates.
- Extensive travel required.
- Other duties as assigned.